Root-knot nematode modulates plant CLE3-CLV1 signaling as a long-distance signal for successful infection

Author:

Nakagami Satoru1ORCID,Notaguchi Michitaka2ORCID,Kondo Tatsuhiko3ORCID,Okamoto Satoru45ORCID,Ida Takanori6ORCID,Sato Yoshikatsu7,Higashiyama Tetsuya8ORCID,Tsai Allen Yi-Lun19ORCID,Ishida Takashi110ORCID,Sawa Shinichiro191011ORCID

Affiliation:

1. Graduate School of Science and Technology, Kumamoto University, Kumamoto 860-8555, Japan.

2. Bioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan.

3. Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan.

4. Graduate School of Science and Technology, Niigata University, Niigata 950-2181, Japan.

5. Japan Science and Technology Agency, Precursory Research for Embryonic Science and Technology, Saitama, 332-0012, Japan.

6. Department of Bioactive Peptides, Frontier Science Research Center, University of Miyazaki, Miyazaki 889-1692, Japan.

7. Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Nagoya 464-8601, Japan.

8. Department of Biological Sciences, Graduate School of Science, University of Tokyo, Tokyo 113-0033, Japan.

9. International Research Center for Agricultural & Environmental Biology, Kumamoto University, Kumamoto 860-8555, Japan.

10. International Research Organization for Advanced Science and Technology (IROAST), Kumamoto University, Kumamoto 860-8555, Japan.

11. Institute of Industrial Nanomaterial (IINA), Kumamoto University, Kumamoto 860-8555, Japan.

Abstract

Plants use many long-distance and systemic signals to modulate growth and development, as well as respond to biotic and abiotic stresses. Parasitic nematodes infect host plant roots and cause severe damage to crop plants. However, the molecular mechanisms that regulate parasitic nematode infections are still unknown. Here, we show that plant parasitic root-knot nematodes (RKNs), Meloidogyne incognita , modulate the host CLAVATA3 (CLV3)/EMBRYO SURROUNDING REGION (CLE)–CLV1 signaling module to promote the infection progression. Plants deficient in the CLE signaling pathway show enhanced RKN resistance, whereas CLE overexpression leads to increased susceptibility toward RKN. Grafting analysis shows that CLV1 expression in the shoot alone is sufficient to positively regulate RKN infection. Together with results from the split-root culture system, infection assays, and CLE3-CLV1 binding assays, we conclude that mobile root-derived CLE signals are perceived by CLV1 in the shoot, which subsequently produce systemic signals to promote gall formation and RKN reproduction.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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